SMPDL3A

Panel	Reviews	Mode of inheritance	Details
Red SMPDL3A in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Sensory Neuropathy
Red SMPDL3A in Pain syndromes Level 2: Neurology and neurodevelopmental disorders Version 0.34 Component of the following Super Panels: Progressive Neurological Conditions	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Sensory Neuropathy

Panel

Reviews

Mode of inheritance

Details

Version 1.1902

review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Neurology and neurodevelopmental disorders
Version 0.34

Component of the following Super Panels:

Progressive Neurological Conditions

review

BIALLELIC, autosomal or pseudoautosomal

2 panels